HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906522Generated: October 30, 2026
2-Acetylamino-5-formyl-4-trifluoromethyl-benzoic acid methyl ester → 2-Acetylamino-5-(1-hydroxy-butyl)-4-trifluoromethyl-benzoic acid methyl ester
https://huagongshe.com/reaction/906522
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Acetylamino-5-formyl-4-trifluoromethyl-benzoic acid methyl ester | HCID 59164423 | — |
| Reactant | HCID 178455855 | HCID 178455855 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Acetylamino-5-(1-hydroxy-butyl)-4-trifluoromethyl-benzoic acid methyl ester | HCID 58532928 | 23.3% |
Reaction Steps
To a solution of 2-acetylamino-5-formyl-4-trifluoromethyl-benzoic acid methyl ester (1.52 g, 5.26 mmol) in absolute Et2O (52 mL), under argon, was added a solution of propylmagnesium chloride (2.0 M in Et2O, 5.3 mL, 11 mmol) over 5 min at 20° C. An immediate crystallisation occurred along with an exotherm. The reaction mixture was cooled to 20° C. using an ice/water bath. The reaction mixture was stirred at r.t. for 1 h then poured onto sat. aq NH4Cl and EtOAc. The pH was adjusted to 7 with sat. aq NH4Cl and the layers were separated. The organic phase was washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by flash column chromatography (25 g silica gel, hexanes/EtOAc (1:0→7:3)) to give product as colorless crystals (409 mg, 23%). m.p.: 97-101° C., ESI-MS: m/z 334 [M+H]+, m/z 332 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012988B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-434d815660814351b0effdc8c7c09ab0 |
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| Source note | uspto-grants-2011_09 |
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